Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28673728 | 1 | 37943401 | intron variant | A/G | snv | 0.40 | 3 | ||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs34651 | 1.000 | 0.040 | 5 | 72848178 | non coding transcript exon variant | C/T | snv | 0.94 | 5 | ||
rs66969865 | 5 | 73124957 | intron variant | C/T | snv | 9.8E-02 | 3 | ||||
rs9623 | 5 | 68301493 | 3 prime UTR variant | T/A;C | snv | 3 | |||||
rs1885486 | 6 | 7695740 | intergenic variant | G/A | snv | 0.40 | 4 | ||||
rs11556924 | 0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 | 21 | ||
rs9314323 | 8 | 26385620 | intron variant | A/G;T | snv | 3 | |||||
rs2277339 | 12 | 56752285 | missense variant | T/G | snv | 0.12 | 0.14 | 10 | |||
rs3218036 | 19 | 29814777 | intron variant | G/A | snv | 0.23 | 3 |